Larry Lowe, IDK if you’ll ever read this. Hope you do. I’ve been dealing with chronic stuff for decades. Been long-C since 2020 & mostly bedridden. Had No vac, but threw off the 1st infection quickly using certain alternatives. The viru$ itself can do what the 💉does, too, depending on the person. Industry workers mean well, but most don’t realize how “owned” everything is, nor how wonky the safety/efficacy Data has become over the past 50 years. But, Imho, & based on experience & training…. Those struggling MIGHT get relief by using certain alternatives. I’ve been trying some, & slowly, they seem to be helping, for the 1st time in 4 years. Cannot risk them disappearing from availability here, because in the States, “witch hunting” still happens, so, won’t risk too much here. There are a few kinds of concentrated nutritive supplements, mostly. Alternative providers might be able to point to some. It takes consistently sticking to protocols over time-these have Not, to my knowledge, been specifically researched for semi-fasting on type A2 organic, pastured, “first food”, + concentrated organic green coffee elements’ effects on the liver that boost glutathione. After just 1 week, my pain levels are noticeably reducing, etc. That is SOMEthing. For all who suffer…I wish you relief & healing!
Just a passing comment purely on behalf of suffers of trigeminal nerve face pain. This can be caused (quite commonly) by poor tooth extractions by your dentists or teeth problems and gum infections in general. Have your teeth checked out. It is quite common for wisdom teeth to be extracted and part of the tooth to remain in the gum, or even for part of the gum (and jaw) to be removed along with the tooth. This can lead to Oroantral fistulas for example - en.wikipedia.org/wiki/Oroantral_fistula - which will irritate the trigeminal nerve and lead to ALL KINDS of horrible symptoms, numbness, migraines, sinus infections, sore throats, halitosis etc. etc. etc. In the case of a fistula - a small operation to close it can be performed, in the case of a tooth remnant - again, a small operation or extraction within the gum. I suspect, problems or infections with the ears could also cause irritation of the trigeminal nerve. Take care.
I should also mention, I am talking about people with MINOR biological conditions here that are caused/triggered by specific DNA. In my case, as the name suggests "psoriatic arthritis" - is related to having prior symptoms of Psoriasis - a simple skin condition. Funnily enough - I've never suffered with any psoriasis in my entire life! Even with psoriatic arthritis now, I only get minor psoriasis on my elbows (although I should mention, during a flair up, all my finger nails and toe nails dropped off and I had major oedema in both leg which felt like 3rd degree burns followed by a good stay in hospital and major arthritic problems - again caused by my own immune system). Anyway, I digress. MY MAIN POINT TO TAKE AWAY IS - The Doctors DON'T KNOW - it took me 5 YEARS! to be diagnosed - and then only because of visible symptoms during a flair up. A little bit of Psoriasis? A little bit of Dermatitis? Maybe it's so minor you don't even have an issue with it - but it may very well indicate that your DNA is prone to go into "major offensive" mode and trigger an attack on your own body. It's a very well known fault in people's DNA - the same fault that triggers Psoriatic Arthritis. Take care. Hope a doctor is reading this as well. They've never really bothered with a treatment of Psoriatic Arthritis. Now they have stuff like "long covid". When I tried to get diagnosed, they refused a diagnosis of "chronic fatigue" through sheer arrogance and disbelief that such a condition could actually exist. Doctors should learn to LISTEN TO PEOPLE - AND BELEIVE WHAT THEY'RE BEING TOLD! PPS: The Mrs suffers with Neuralgia - migraines and pain in the side of the face with the trigeminal nerve. She ALSO suffers with minor Dermatitis on her finger. I think she should be treated with immunosuppressors as I believe her dermatitis is the primary origin of this immune reaction, but they try to treat the migraines which are the "symptoms". If you want some relief from nerve pain - you should be taking pregabalin and codeine. Be very careful though, both are addictive (I've taken them both now for 25 years, so a bit late for me) but the pregabalin is worse to come off than the codeine. Only take them for occasional relief of the symptoms - then treat the cause of the symptoms with immunosuppressors. Bye! Good Luck!
@@davegriff1593 Yeah, pregabalin is pretty heavy depending on dosage. It's something that should either be take at night/evening or at a low dose (50mg) during the day. Again, I would only recommend it if you feel like the symptoms are really too much to cope with and you need something to relieve it (starts working in 30 minutes). 25 to 50mg - probably no more than twice a day, or 100mg once a day in an evening. You do build up a tolerance if you take them long term, but that would lead to addiction. Always better to treat the condition itself ASAP so your not taking them longer than you have to. Same with coedine.
I pray that you will get better Your not alone mom had a mini stroke 5/6 weeks after the second shot in Nov , was generally unwell through Christmas . Stroke in Jan
As a sufferer of Psoriatic Arthritis since 29, it is pretty clear to me what has happened and what the treatment should include Larry. Essentially, there is NOTHING more powerful and potentially destructive in the human body than your own immune system - and in your case, that has what has effectively been triggered against your own body by the Covid booster. I have a genetic condition - Psoriatic Arthritis. When I was 29, in 1999, I got flu. I hadn't been ill a day in my life and was fit and active. I never really recovered from this flu. It trigger an immune response that caused my own immune system to attack my own body, identifying any (even minor) damage or wear as a potential infection - causing my own immune system to attack my own body. When your immune system attacks you in this way, like having a flu, you feel constantly tired, exhausted and in pain (besides flu like systems, in my particular case - psoriatic arthritis - it attacks my joints). But it ALSO attacks nerves in a lot of cases, the sciatic nerve - trigeminal nerves, etc. etc. Ask your doctor about immune system suppressors, like Amgevita and Methotrexate: www.drugs.com/uk/amgevita.html www.nhs.uk/medicines/methotrexate In your particular case, I should imagine you would only need to take it for a year or so until the symptoms fall off, or if you continue to have flair ups. You need to train your immune system to stop attacking your own body - essentially telling it to "chill the f*ck out". Take care Larry, I hope you get better my friend and that this information helps you in some way.
i have a friend who has this on her face, her right trigeminal nerve is not working and my friend suspects it is related to the booster she had. Also, this is not a rare condition as her neurologist has said that she has seen many ,many more neurological patient suffering from it... a sensory type of Bells Palsy..
Larry, I have also been diagnosed with the same condition after the covid jab. I to went via a private neurologist. It started the day after the injection. It is made worse by the cold and is now quite painful now the temp has dropped. Anti depressants helped but unfortunately they affected me other ways so I stopped. However, I did get some relief last winter using capsium cream, it seems to send your nerves into overdrive and blocks the pain, however it does have other issues but they are bearable. I have not applied it yet as I am saving it for the really cold weather. My Dr gave me a prescription for it but chemusts do not stock it due to Brexit ? but , I got it from Ebay, I will send you the link if you want it.
Hi Larry My partner and I also saw your story and would like to try helping if you’re able to share your contact info. We can also contact the reporter if it’s easier. Our heart is with you.
Larry - I saw your story on BBC news app tonight. I have written to the reporter and asked her to pass on to you my sincere thoughts. I'm nowhere near as bad as you but I really feel for you.
Thank you so much for posting this! This is now my favorite version of CWH. I have always enjoyed Daoiri's music and have been slowly getting better on my octave mandolin (closest thing I have to a Bouzouki). His style, along with Andy Irvine's, is an inspiration to me. :-) Capt. Blackheart Charlie, s/v Aurora Key West
Excellent to see this progressive farming system in Tyrone. Strange too to think that back in the 50’s and 60’s we were taught about the principles of this rotational style of farming at the CBS… Nicely filmed too but it would also have been nice to see a bit more about the overall Community .
Good on you Daori .I agree totally with what you say about taking a song and giving it a personal touch. I do this too with most of my songs. Im a great fan - in fact it`s your fault that I started playing the Irish Bouzouki - I saw The Creggan white Hare and was hooked. I can do a passable version of that song now and Im working on Blackwater side which you did at the Witches Hat 🙂
Connor, you really have one of the most beautiful voices I have ever heard, you literally brought to ta tears, my nephew sent me a clip of you, he knows I'm a mad Elvis fan, I believe he thought you, Mr Hoban, or if friends with your Dad, when I visit him next. In Tyrone I hope I can see you live.. never give up,,, you did your grandad proud. X
